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1.
Indian J Hum Genet ; 2005 May; 11(2): 105-107
Article de Anglais | IMSEAR | ID: sea-143339

RÉSUMÉ

BACKGROUND : Cytogenetics study using cultured T-lymphocytes derived from peripheral blood is the easiest way to study human chromosome complement and it is also an excellent method to study chromosomal abnormalities: either structural or numerical. The structural chromosomal abnormalities include translocations, deletions, duplications, ring chromosomes and isochromosomes. AIMS : Cases presenting with multiple congenital anomalies, mental retardation, pregnancy wastage or abnormalities in sexual function are referred to the Division of Human Genetics to rule out chromosomal anomalies. METHODS AND MATERIALS : A total of 70 cases with multiple congenital anomalies, mental retardation, pregnancy wastage or abnormalities in sexual function were studied. About 72 h cultured peripheral lymphocytes subjected to GTG banding were analyzed to look at the chromosome profile. RESULTS : Out of 70 cases of reciprocal translocation, single cell translocations were seen in ten cases (three females; seven males). Looking at the case profile, it was seen that they were referred for mental retardation, bad obstetric history and hypogonadism. It was seen that seven cases (70%) had t(7;14), two (20%) had complex translocations: t(X;9;8) and t(2;10;11), and one (10%) had t(4;21). CONCLUSIONS : Depending on the phenotype, the patients were informed of their abnormality and the need for a look out for the development of any associated problems.

2.
J Indian Med Assoc ; 1998 Nov; 96(11): 335-7
Article de Anglais | IMSEAR | ID: sea-103742

RÉSUMÉ

The effect of consanguinity on the non-disjunction mechanism in Down's syndrome, was examined in 417 cytogenetically confirmed Down's syndrome patients. The incidence of parental and grandparental consanguinity was 17.5% (n = 73), while that of only parental consanguinity was 17.2% (n = 71). First cousin marriages occurred more frequently, than uncle-niece and 2nd cousin marriages. With regard to parental age, only the mean age difference between consanguineous couples significantly differed from non-consanguineous couples. The inbreeding coefficient did not differ between trisomy 21 and translocation Down's families. From this study, it is concluded that consanguinity does not predispose to Down's syndrome.


Sujet(s)
Adulte , Loi du khi-deux , Enfant , Enfant d'âge préscolaire , Consanguinité , Syndrome de Down/épidémiologie , Femelle , Enquêtes de santé , Humains , Incidence , Inde/épidémiologie , Nourrisson , Nouveau-né , Mâle , Parents , Facteurs de risque , Études par échantillonnage , Répartition par sexe , Statistique non paramétrique
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